posted on 2022-05-23, 16:09authored byJinglun Du, Andrea Fiorani, Taichi Inagaki, Atsushi Otake, Michio Murata, Miho Hatanaka, Yasuaki Einaga
By means of an initial
electrochemical carbon dioxide reduction
reaction (eCO2RR), both the reaction current and Faradaic
efficiency of the eCO2RR on boron-doped diamond (BDD) electrodes
were significantly improved. Here, this effect is referred to as the
self-activation of BDD. Generally, the generation of carbon dioxide
radical anions (CO2•–) is the
most recognized pathway leading to the formation of hydrocarbons and
oxygenated products. However, the self-activation process enabled
the eCO2RR to take place at a low potential, that is, a
low energy, where CO2•– is hardly
produced. In this work, we found that unidentate carbonate and carboxylic
groups were identified as intermediates during self-activation. Increasing
the amount of these intermediates via the self-activation process
enhances the performance of eCO2RR. We further evaluated
this effect in long-term experiments using a CO2 electrolyzer
for formic acid production and found that the electrical-to-chemical
energy conversion efficiency reached 50.2% after the BDD self-activation
process.